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Clinical Research Associate Trainee Jobs in Raleigh, NC

IQVIA

Clinical Research Associate

Durham, NC

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site

The Sr. Clinical Research Associate will serve as a key operational partner, acting as the primary point of contact for assigned external study sites, investigators, and collaborators while ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site +1

The Sr. Clinical Research Associate will serve as a key operational partner, acting as the primary point of contact for assigned external study sites, investigators, and collaborators while ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC · On-site

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC · On-site

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA, Inc.

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Clinical Research Associate

Durham, NC

$87K - $182K/yr

Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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Clinical Research Associate Trainee information

See Raleigh, NC salary details

$12

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$53

How much do clinical research associate trainee jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research associate trainee in Raleigh, NC is $30.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $40.43 per hour, depending on experience, location, and employer.

What is a clinical research associate trainee?

Clinical Research Associate (CRA) Trainees are entry-level professionals who assist in the monitoring, coordination, and administration of clinical trials. They work under the supervision of experienced CRAs to ensure that clinical research studies comply with regulatory requirements, protocols, and ethical standards. CRA Trainees are typically involved in site visits, data verification, documentation, and communication between study sites and sponsors. Their role serves as a foundation for advancing to more senior CRA positions within the clinical research field.

What are the key skills and qualifications needed to thrive as a clinical research associate trainee, and why are they important?

To thrive as a Clinical Research Associate Trainee, you need a solid background in life sciences or a related field, strong organizational skills, and keen attention to detail. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and relevant certifications such as GCP training are typically required. Excellent communication, problem-solving abilities, and adaptability are important soft skills for building relationships with site staff and ensuring protocol compliance. These skills and qualities are vital for maintaining data integrity, patient safety, and regulatory adherence throughout the clinical trial process.

What types of projects and studies can a clinical research associate trainee expect to work on during their first year?

As a Clinical Research Associate Trainee, you will typically be involved in assisting with a variety of clinical trials, ranging from early-phase (Phase I/II) to later-phase (Phase III/IV) studies. Your responsibilities may include site monitoring, verifying that clinical data is accurately recorded, and ensuring compliance with regulatory guidelines. You'll often work closely with senior CRAs, study coordinators, and investigators, allowing you to gain hands-on experience with protocols and Good Clinical Practice (GCP) standards. This exposure prepares you for more independent monitoring roles as you progress in your career.

What is the difference between Clinical Research Associate Trainee vs Clinical Research Associate?

AspectClinical Research Associate TraineeClinical Research Associate
Required CredentialsOften entry-level, may require a bachelor's degree in life sciences or related fieldRequires relevant experience, often a bachelor's degree and certification
Work EnvironmentTraining programs, supervised settings, clinical trial sitesIndependent monitoring at clinical sites, data review, regulatory compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms during training phaseEstablished professionals working in similar organizations

The Clinical Research Associate Trainee is an entry-level position focused on learning and training, often requiring minimal experience. In contrast, a Clinical Research Associate is a more experienced role responsible for monitoring clinical trials independently. The trainee role serves as a stepping stone toward becoming a full Clinical Research Associate.

Clinical Research Associate Trainee jobs near you
Infographic showing various Clinical Research Associate Trainee job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $63,772 per year, or $30.7 per hour.

Clinical Research Associate II / Senior Clinical Research Associate

410 ICR United States USA

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago

Job description

North America | Remote | Sponsor-Dedicated (FSP) Opportunities

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.

About the Opportunity

As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.

Depending on your experience level, you may:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure protocol compliance, patient safety, data quality, and regulatory adherence
  • Build strong relationships with investigative sites and key stakeholders
  • Identify and proactively resolve site and study issues
  • Collaborate with cross-functional teams to support successful study delivery
  • Support inspection readiness and high-quality study execution
  • Mentor and guide less experienced CRAs (Senior CRA level)

What We're Looking For

CRA II

  • Bachelor's degree in a scientific, healthcare, or related field
  • Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
  • Ability to work independently while collaborating effectively across teams

Senior CRA

  • Significant clinical monitoring experience across multiple studies and sites
  • Advanced knowledge of clinical trial processes, regulations, and site management
  • Proven ability to manage priorities and drive study quality independently
  • Experience mentoring or supporting other CRAs is advantageous

For all applicants

  • Strong communication and relationship-building skills
  • Willingness to travel as required
  • Passion for advancing clinical research and improving patient outcomes

When you join ICON Strategic Solutions, you gain the best of both worlds:

  • Work within dedicated sponsor environments
  • Build expertise with leading global pharmaceutical and biotechnology companies
  • Access diverse opportunities across multiple therapeutic areas
  • Benefit from ICON's global scale, career development, and support network
  • Join a culture focused on innovation, collaboration, and patient impact
  • Competitive compensation and benefits package

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply